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My MG Story: Victoria Discusses Life and Work with Myasthenia Gravis
Nine years ago, Victoria woke up with MG symptoms. She shares her experience with diagnosis and treatment in a small town.
LATEST FROM THE MGFA INSIDER BLOG
Running the NYC Marathon for a World without Myasthenia Gravis
MGFA sat down with MG patient Julie and her boyfriend, Zack, who is
running the marathon for MG awareness, to talk about why supporting the MGFA matters to them
both.
My MG Story: Getting My Smile Back
As a new mom, Hannah Ensor faced challenging and confusing medical
symptoms.
Requesting Accommodations for Myasthenia Gravis at Work
Tips for ensuring you are seen, heard, and
accommodated.
Triumphant Summa Cum Laude
What it’s like to go to college while battling
myasthenia gravis
I Want to Throw a Pity Party, But No One Will Come
Greg Josephs leans into a positive life to manage myasthenia
gravis.
This Isn’t My Story, But It Is My Life: My Father Has MG
I was five years old, and I didn't understand what was
going on. All I knew was that I was scared.
A Tribute to Stan Way: A dedicated Volunteer Leader in the MG Community
Remembering a visionary educator, community builder,
and champion of the internet’s power to create connections.
Myasthenia Gravis Considerations in Dentistry
On August 17, dentist and MG patient Dr. Gene Cassagrande led a Wellness Webinar focused on having a successful dentist visit when you have myasthenia gravis. Dr. Cassagrande practiced dentistry for 30 years before transitioning into a role as a medical device salesperson. With his deep knowledge of dentistry and his lived experience with MG, […]
Targeting B cells may help people with MuSK Myasthenia Gravis
“For me, precision medicine has always been the holy
grail of what we’re trying to
achieve.”
Finding a Place to Stay When You Travel for Medical Care
Options for discounted lodging for patients and their
families.